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Conference Paper: Electrochromic materials using mechanically interlocked molecules

TitleElectrochromic materials using mechanically interlocked molecules
Authors
Keywords[2]catenanes
Carge-transfer complex
Electrochromism
Electronic paper display
Interlocked molecules
Issue Date2008
Citation
Science and Technology of Advanced Materials, 2008, v. 9, n. 1, article no. 014104 How to Cite?
AbstractRecent investigations on the design and synthesis of electrochromic materials based on switchable three-station [2]catenanes are summarized. The reasoning and preliminary experiments behind the design of electrochemically controllable red-green-blue (RGB), donor-acceptor [2]catenanes are presented. A basis for color generation is discussed in which the tetracationic cyclophane, cyclobis(paraquat-p-phenylene), serves as the π-electron deficient ring which circumrotates between three π-electron rich recognition sites within a macrocyclic polyether, generating the three different colors (RGB) based on the different charge transfer interactions between the tetracationic cyclophane and recognition sites based on 1,5-dioxynaphthalene (R), tetrathiafulvalene (G) and benzidine (B). Issues relating to the realization of an RGB [2]catenane are raised and discussed: they include (i) color tuning, (ii) thermodynamic considerations, (iii) electrochemistry on model compounds, (iv) molecular design, (v) the electrochemical behavior of three-station [2]catenanes and (vi) electrochromism in polymer gel matrices. Finally, the challenges that need to be met in the future if the ideal RGB catenane is to be prepared, are outlined. © 2008 National Institute for Materials Science.
Persistent Identifierhttp://hdl.handle.net/10722/333606
ISSN
2023 Impact Factor: 7.4
2023 SCImago Journal Rankings: 0.972
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorIkeda, Taichi-
dc.contributor.authorStoddart, James Fraser-
dc.date.accessioned2023-10-06T05:20:58Z-
dc.date.available2023-10-06T05:20:58Z-
dc.date.issued2008-
dc.identifier.citationScience and Technology of Advanced Materials, 2008, v. 9, n. 1, article no. 014104-
dc.identifier.issn1468-6996-
dc.identifier.urihttp://hdl.handle.net/10722/333606-
dc.description.abstractRecent investigations on the design and synthesis of electrochromic materials based on switchable three-station [2]catenanes are summarized. The reasoning and preliminary experiments behind the design of electrochemically controllable red-green-blue (RGB), donor-acceptor [2]catenanes are presented. A basis for color generation is discussed in which the tetracationic cyclophane, cyclobis(paraquat-p-phenylene), serves as the π-electron deficient ring which circumrotates between three π-electron rich recognition sites within a macrocyclic polyether, generating the three different colors (RGB) based on the different charge transfer interactions between the tetracationic cyclophane and recognition sites based on 1,5-dioxynaphthalene (R), tetrathiafulvalene (G) and benzidine (B). Issues relating to the realization of an RGB [2]catenane are raised and discussed: they include (i) color tuning, (ii) thermodynamic considerations, (iii) electrochemistry on model compounds, (iv) molecular design, (v) the electrochemical behavior of three-station [2]catenanes and (vi) electrochromism in polymer gel matrices. Finally, the challenges that need to be met in the future if the ideal RGB catenane is to be prepared, are outlined. © 2008 National Institute for Materials Science.-
dc.languageeng-
dc.relation.ispartofScience and Technology of Advanced Materials-
dc.subject[2]catenanes-
dc.subjectCarge-transfer complex-
dc.subjectElectrochromism-
dc.subjectElectronic paper display-
dc.subjectInterlocked molecules-
dc.titleElectrochromic materials using mechanically interlocked molecules-
dc.typeConference_Paper-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1088/1468-6996/9/1/014104-
dc.identifier.scopuseid_2-s2.0-49049107361-
dc.identifier.volume9-
dc.identifier.issue1-
dc.identifier.spagearticle no. 014104-
dc.identifier.epagearticle no. 014104-
dc.identifier.isiWOS:000257128300014-

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